S. Fattore

Temperature‐programmed capillary electrophoresis for the analysis of high‐melting point mutants in thalassemias

P. Righetti, C. Gelfi, M. Travi, 1997, Electrophoresis.

Genetic interactions in thalassemia intermedia: analysis of beta-mutations, alpha-genotype, gamma-promoters, and beta-LCR hypersensitive sites 2 and 4 in Italian patients.

M. Cappellini, C. Camaschella, A. Roetto, 1995, American journal of hematology.

Genetic interactions in thalassemia intermedia: Analysis of β‐Mutations, α‐Genotype, γ‐Promoters, and β‐LCR hypersensitive sites 2 and 4 in Italian patients

M. Cappellini, C. Camaschella, A. Roetto, 1995 .

Mutation and Polymorphism Report

N. Mirra, P. Primignani, R. Ghilardi, 1999 .

A novel −27A>G point mutation in the beta globin gene

N. Mirra, P. Primignani, R. Ghilardi, 1999 .

A homozygous missense arginine to histidine substitution at position 482 of the β-galactosidase in an Italian infantile GM1-gangliosidosis patient

S. Brocca, E. Gianazza, C. Danesino, 1992, Human Genetics.

A pilot study of factors associated with glycaemic control in adults with Type 1 diabetes mellitus on insulin pump therapy

B. Shadbolt, K. Wright, R. Frampton, 2016, Diabetic medicine : a journal of the British Diabetic Association.

First-trimester fetal screening of cystic fibrosis in low-risk population

B. Brambati, L. Tului, C. Férec, 1993, The Lancet.